P N Ray|M L Pearson - JoVE Visualize

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British Medical Bulletin|July 1, 1989

Myogenic regulation of dystrophin gene expressionH J Klamut, E E Zubrzycka-Gaarn, D E Bulman, et al.

Cytogenetic and Genome Research|April 1, 2006

New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndromeA C Smith, T Rubin, C Shuman, et al.

Neurogenetics|June 5, 2013

Autosomal recessive hereditary spastic paraplegia-clinical and genetic characteristics of a well-defined cohortG Yoon, B Baskin, M Tarnopolsky, et al.

Annals of Internal Medicine|August 1, 1992

Nosocomial transmission of multidrug-resistant Mycobacterium tuberculosis. A risk to patients and health care workersM L Pearson, J A Jereb, T R Frieden, et al.

Gene|November 14, 1998

Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin geneJ C McNaughton, D J Cockburn, G Hughes, et al.

JAMA|October 14, 1992

Differences in quality of care for hospitalized elderly men and womenM L Pearson, K L Kahn, E R Harrison, et al.

American Journal of Human Genetics|June 1, 1997

Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy numberP E McAndrew, D W Parsons, L R Simard, et al.

Neurogenetics|March 25, 2000

Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7C F Rochette, L C Surh, P N Ray, et al.

Archives of Internal Medicine|October 23, 1995

Epidemiology of do-not-resuscitate orders. Disparity by age, diagnosis, gender, race, and functional impairmentN S Wenger, M L Pearson, K A Desmond, et al.

The Journal of Biological Chemistry|December 10, 1984

Isolation and sequence analysis of cDNA clones coding for rat skeletal muscle creatine kinaseP A Benfield, R A Zivin, L S Miller, et al.

Pageof 13

Showing results (91-100 of 129) with videos related to

Sort By:

Pageof 13

British Medical Bulletin|July 1, 1989

Myogenic regulation of dystrophin gene expressionH J Klamut, E E Zubrzycka-Gaarn, D E Bulman, et al.

Cytogenetic and Genome Research|April 1, 2006

New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndromeA C Smith, T Rubin, C Shuman, et al.

Neurogenetics|June 5, 2013

Autosomal recessive hereditary spastic paraplegia-clinical and genetic characteristics of a well-defined cohortG Yoon, B Baskin, M Tarnopolsky, et al.

Annals of Internal Medicine|August 1, 1992

Nosocomial transmission of multidrug-resistant Mycobacterium tuberculosis. A risk to patients and health care workersM L Pearson, J A Jereb, T R Frieden, et al.

Gene|November 14, 1998

Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin geneJ C McNaughton, D J Cockburn, G Hughes, et al.

JAMA|October 14, 1992

Differences in quality of care for hospitalized elderly men and womenM L Pearson, K L Kahn, E R Harrison, et al.

American Journal of Human Genetics|June 1, 1997

Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy numberP E McAndrew, D W Parsons, L R Simard, et al.

Neurogenetics|March 25, 2000

Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7C F Rochette, L C Surh, P N Ray, et al.

Archives of Internal Medicine|October 23, 1995

Epidemiology of do-not-resuscitate orders. Disparity by age, diagnosis, gender, race, and functional impairmentN S Wenger, M L Pearson, K A Desmond, et al.

The Journal of Biological Chemistry|December 10, 1984

Isolation and sequence analysis of cDNA clones coding for rat skeletal muscle creatine kinaseP A Benfield, R A Zivin, L S Miller, et al.

Pageof 13